NDC 80569-101 Crystal Flush Maximum Strength Anti-fungal Formula
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What is NDC 80569-101?
What are the uses for Crystal Flush Maximum Strength Anti-fungal Formula?
Which are Crystal Flush Maximum Strength Anti-fungal Formula UNII Codes?
The UNII codes for the active ingredients in this product are:
- TOLNAFTATE (UNII: 06KB629TKV)
- TOLNAFTATE (UNII: 06KB629TKV) (Active Moiety)
Which are Crystal Flush Maximum Strength Anti-fungal Formula Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- ALMOND OIL (UNII: 66YXD4DKO9)
- CITRONELLA OIL (UNII: QYO8Q067D0)
- LAVENDER OIL (UNII: ZBP1YXW0H8)
- TEA TREE OIL (UNII: VIF565UC2G)
- JOJOBA OIL (UNII: 724GKU717M)
- CLOVE OIL (UNII: 578389D6D0)
- AZADIRACHTA INDICA SEED OIL (UNII: 4DKJ9B3K2T)
- .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
What is the NDC to RxNorm Crosswalk for Crystal Flush Maximum Strength Anti-fungal Formula?
- RxCUI: 313423 - tolnaftate 1 % Topical Solution
- RxCUI: 313423 - tolnaftate 10 MG/ML Topical Solution
* Please review the disclaimer below.
Patient Education
Tolnaftate
Tolnaftate stops the growth of fungi that cause skin infections, including athlete's foot, jock itch, and ringworm. This medication is sometimes prescribed for other uses; ask your doctor or pharmacist for more information.
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* Please review the disclaimer below.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".